A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062077



Internal ID19151296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27596469hg38UCSC Ensembl
Innerchr19:27747981..28087377hg19UCSC Ensembl
Innerchr19:32439821..32779217hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38339397
hg19339397
hg18339397
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3498n100
Supporting Variantsnssv3572025, nssv3572026, nssv3572027, nssv3572028
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062077
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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